This two-group clinical trial utilized a pretest-posttest design. The statistical population included all cancer patients aged 6 - 12 years admitted to the Hematology Ward of Ali Ibn Abitalib Hospital of Zahedan for intra-spinal injection of chemotherapy drugs in 2017. Based on the study by Vosoghi et al. (
10) and considering the mean SaO
2 in the intervention and control groups, the test power of 80%, and the significance of 0.05, the authors estimated 39 individuals for each group. This was increased to 45 in order to ensure the adequacy of the sample size. After obtaining an introduction letter from the vice chancellor for research and information technology of Zahedan University of Medical Sciences and acquiring the required permits (code of ethics issued by the Ethics Committee, IR.ZAUMS, REC.1396.110), the researcher began the sampling process. Thus, we selected 90 eligible cancerous children aged 6 - 12 years who had been admitted to the abovementioned hospital for outpatient chemotherapy through convenience sampling. After explaining the goals of the study and obtaining informed consent from the parents, the researcher enrolled the subjects and next randomized them into the intervention (n = 45) and control (n = 45) groups.
The inclusion criteria were an intra-spinal injection prescription for the child by the specialist physician; orientation to time, place, and person as determined via oral questions designed to test the child’s alertness to person (identifying the mother), the time of day and night, and his/her location in the hospital; ability to communicate verbally; lack of seizure or any life-threatening emergency (heart disease, acute respiratory disorder, etc.); lack of taking painkillers via intra-spinal injection before starting chemotherapy; and completion of the consent form by parents or the legal guardian. On the other hand, the exclusion criteria were the lack of cooperation by the child or his/her family at each stage of research, child’s restlessness and intolerance of the research conditions, and death of the child during the study. The data collection instruments included a form for recording personal information, another form for recording physiological indices and finally, a pain assessment questionnaire. Personal and disease information included age, sex, the frequency of intra-spinal injection of chemotherapy drug, duration of disease, heart rate, and arterial oxygen saturation of children before and immediately after the intra-spinal injection. A pulse oximetry device (manufactured by Nonin Medical Inc.) along with a pediatric probe was used for measuring the heart rate and SaO
2. A standard Oucher scale was employed to evaluate the pain severity. This tool was developed by Beyer (1984) to assess the severity of pain in children aged 3 to 12 years. It is one of the most reliable and widely used scales for the self-report of pain that uses the photographs of children’s face in painful situations (
10,
11). This tool is used by pediatric health practitioners around the world, and studies have established its content and construct validity (
11). It uses different photographs of children’s face in normal and upset moods taken from real children while experiencing real pain in hospitals. For use in children who are not capable of counting, this tool consists of six photographs that represent varying degrees of pain set vertically from bottom to up. The photographs are graded one to six, with one showing no pain, two representing mild pain, three and four standing for moderate pain, five denoting severe pain, and six indicating the most severe pain which the child goes through (
11). A vertical table with numbers 0 - 100 is also used on the left side of the photographs. This numerical measure is used for children who are able to count. In this table, zero suggests no pain, one to 29 signify mild pain, 30 to 69 refer to moderate pain, 70 to 99 indicate severe pain, and 100 represents the highest imaginable pain (
12).
The distraction intervention was implemented using an animated movie, a monitor, and music with headphones. After the physician’s order for intra-spinal injection of chemotherapy drug was checked in both groups, the heart rate and SaO2 of the subjects were gauged using the Nonin pulse oximeter when the child was sitting on the bed. In order to reduce children’s anxiety and attract their attention, the pulse oximeter was first connected to the researcher’s finger. After giving a full explanation and gaining their confidence, the researcher attached the device to the child’s finger. Thus, the heart rate and the degree of SpO2 were recorded in the form of physiological indices before injection. Then, children in the intervention group were asked to choose one out of three suggested cartoons: Shekarestan (Sugarland), Sponge Bob, and Tom & Jerry, broadcast by the Islamic Republic of Iranian Broadcasting. The steps of injection preparation included providing the injection kit, wearing sterile gloves by the physician, positioning the patient (sitting and forward head posture), disinfecting the injection site, and performing the injection. This procedure, lasting 10 minutes, was the same for all patients. During the injection period, the child watched his/her chosen cartoon from the monitor, accompanied by music listened through SONY headphones. This was sustained in the intervention group until the end of the injection, i.e. applying the bandage and pasting it. The duration of injection was calculated from the moment of needle penetration to pasting the injection site. Immediately after pasting, the heart rate and arterial oxygen saturation of both groups were re-evaluated and recorded in the form of physiological indices after injection.
The control group received routine care procedures. Ten minutes after chemotherapy and before making any intervention, the children were asked about the severity of pain caused by injection using the Oucher device. Specifically, they were encouraged to point to a number indicating the severity of their pain. The related number was then recorded. The assessment of pain and physiological responses, as well as the distraction intervention, was performed individually for each child.
Data were analyzed by SPSS version 20. In the descriptive section, frequency and percentage were used. In the inferential part, independent and paired t tests were employed. The chi square test was utilized to compare the frequency of qualitative variables. Moreover, the Fisher exact test and Kolmogorov-Smirnov test were adopted to assess the normality of data. The significance level was considered less than 0.05.